Fan W F, Wei X, Shukla H, Parimoo S, Xu H, Sankhavaram P, Li Z, Weissman S M
Boyer Center for Molecular Medicine, Yale University School of Medicine, New Haven, Connecticut 06510.
Genomics. 1993 Sep;17(3):575-81. doi: 10.1006/geno.1993.1374.
Identification of transcribed sequences by cDNA selection is a potentially rapid and efficient way of scanning large genomic DNA fragments for the presence of genes. To evaluate this approach further, we have applied it to three yeast artificial chromosomes (YACs) and examined the products obtained from a total of about 1100 kb from two regions of the human major histocompatibility complex (MHC). One YAC was derived from an extensively studied portion of the Class II region of the MHC. The cDNAs recovered from this YAC included representatives of the previously described genes as well as one or more cDNA clones not described in the databases. A second YAC spanned about 330 kb of DNA surrounding the Class I gene HLA-A. In addition to Class I clones, 10 distinct cDNA products were identified from this YAC. A third YAC contained about 700 kb of human DNA, including 260 kb of overlap with the second YAC, and recovered an additional cDNA complementary to YAC B30 H3 DNA. Overall, the method is shown to be able to detect very scarce cDNAs and to detect a large fraction of coding sequences in YAC clones. Advantages and limitations of the approach are discussed.
通过cDNA筛选鉴定转录序列是一种潜在的快速有效的方法,可用于扫描大型基因组DNA片段中是否存在基因。为了进一步评估这种方法,我们将其应用于三个酵母人工染色体(YAC),并检测了从人类主要组织相容性复合体(MHC)两个区域总共约1100 kb的片段中获得的产物。一个YAC来自MHC II类区域中经过广泛研究的部分。从这个YAC中回收的cDNA包括先前描述的基因的代表以及数据库中未描述的一个或多个cDNA克隆。第二个YAC跨越围绕I类基因HLA - A的约330 kb DNA。除了I类克隆外,从这个YAC中还鉴定出10种不同的cDNA产物。第三个YAC包含约700 kb的人类DNA,包括与第二个YAC重叠的260 kb,并回收了与YAC B30 H3 DNA互补的另一个cDNA。总体而言,该方法被证明能够检测到非常稀少的cDNA,并能检测到YAC克隆中的大部分编码序列。文中讨论了该方法的优点和局限性。